Participant Recruitment

Accelerate recruitment and ‘first patient in’ time

Get started

Participant Recruitment

Accelerate recruitment and ‘first patient in’ time

Get started

Participant Recruitment

Accelerate recruitment and ‘first patient in’ time

Get started

Streamlined user journeys help accelerate time to “first patient in” and get your trial up and running with minimal fuss.

Fully-integrated screening and consent enable faster set-up and enrollment. Our DeTAP atrial fibrillation trial recruited 94% of participants in less than two weeks and maintained an 86% retention rate.

Streamlined user journeys help accelerate time to “first patient in” and get your trial up and running with minimal fuss.

Fully-integrated screening and consent enable faster set-up and enrollment. Our DeTAP atrial fibrillation trial recruited 94% of participants in less than two weeks and maintained an 86% retention rate.

Streamlined user journeys help accelerate time to “first patient in” and get your trial up and running with minimal fuss.

Fully-integrated screening and consent enable faster set-up and enrollment. Our DeTAP atrial fibrillation trial recruited 94% of participants in less than two weeks and maintained an 86% retention rate.

Streamlined user journeys help accelerate time to “first patient in” and get your trial up and running with minimal fuss.

Fully-integrated screening and consent enable faster set-up and enrollment. Our DeTAP atrial fibrillation trial recruited 94% of participants in less than two weeks and maintained an 86% retention rate.

Powering digital-first clinical research

eConsent

eCOA/ePRO

Telemedecine

Connected devices

Seamless set up and go

Maximise participant sign-ups and minimise dropouts with an uninterrupted screening-to-consent process. Invite participants by email directly from the platform and get them up and running quickly with our easy-to-use, step-by-step onboarding module featuring efficient electronic ID verification.

Comprehensive support for multiple market recruitment strategies

The Huma platform is ready to deploy immediately in 80+ countries across the US, Europe, China, Middle East, Southeast Asia, and more. We’re device and cloud-agnostic for the widest possible global deployment flexibility. We have the ability to recruit participants globally via sites, central participant hubs and recruitment marketing campaigns.

Regulatory, safety and compliance

Regulatory compliance
International medical device standards
QMS & info security management
Technical documentation
Regulatory compliance
International medical device standards
QMS & info security management
Technical documentation
Regulatory
compliance
International medical device standards
QMS & info security management
Technical documentation
Regulatory compliance
International medical device standards
QMS & info security management
Technical documentation

Integrated support and expert team

Huma’s experienced team is on-hand to ensure your therapeutic trial is set up to your exact requirements. Our fully-regulated platform can be deployed across multiple countries and offers reliability and a high degree of user acceptance at scale.

Integrated support and expert team

Huma’s experienced team is on-hand to ensure your therapeutic trial is set up to your exact requirements. Our fully-regulated platform can be deployed across multiple countries and offers reliability and a high degree of user acceptance at scale.

Take the next step

Tell us what you’re working on and what you need from Huma to move forward.

Take the next step

Tell us what you’re working on and what you need from Huma to move forward.